[9B1-9B1];[9D3-9D3];
A set of isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Initial core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.
9B1;9D3
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}nejEP1149&P{EP}nejEP1179 and P{EP}α-Man-IEP1628&P{EP}α-Man-IEP1307 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}PPP4R2rEP307 and P{EP}rasEP1235&P{EP}rasEP1427